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Heckscher, E. S.

Publications and source records attributed to Heckscher, E. S..

2 recordsLinked to original sources

Neural birth time and somatosensory circuit assembly are linked by Robo3 regulation of dendrite morphology

Neural circuit wiring requires a remarkable level of precision, as thousands of neurons generate millions of synapses in distinct configurations. While neural circuits are known to be shaped by both neural birth timing and multiple classes of guidance molecules, the relationship between the two and how they coordinate circuit assembly has yet to be evaluated. Leveraging the well-defined stem cell lineages of the Drosophila embryonic nerve cord, we investigate how Roundabout (Robo) guidance receptors are regulated by neural birth timing to establish neural morphology and function for circuit assembly. Our data reveal that Robo receptor expression in neurons is tightly linked to neural birth timing and controlled by temporal transcription factors. Notably, we identify a Robo3 guidance receptor code that is pivotal for assembly of somatosensory circuits, distinguishing stretch-detecting PNS neurons and late-born EL interneurons (lacking Robo3) from vibration detecting PNS neurons and early-born EL interneurons (expressing Robo3). These insights propose a shared guidance receptor code connecting neural birth timing to circuit assembly, providing a molecular foundation for developmental wiring specificity. HighlightsO_LIRobo3 is enriched in early-born neurons and requires Pdm and Castor for normal expression C_LIO_LIClassic temporal identity markers and Robo3 are differentially regulated C_LIO_LIIn interneurons, Robo3 is required for dendrite positioning and branching C_LIO_LIA shared Robo code is used by synaptic partners from different developmental origins C_LI

developmental biology↗

Sequential addition of neuronal stem cell temporal cohorts generates a feed-forward circuit in the Drosophila larval nerve cord

Understanding how circuits self-assemble starting from neuronal stem cells is a fundamental question in developmental biology. Here, we addressed how neurons from different lineages wire with each other to form a specific circuit motif. To do so, we combined developmental genetics--Twin spot MARCM, Multi-color Flip Out, permanent labeling--with circuit analysis--calcium imaging, connectomics, and network science analyses. We find many lineages are organized into temporal cohorts, which are sets of lineage-related neurons born within a tight time window, and that temporal cohort boundaries have sharp transitions in patterns of input connectivity. We identify a feed-forward circuit motif that encodes the onset of vibration stimuli. This feed-forward circuit motif is assembled by preferential connectivity between temporal cohorts from different neuronal stem cell lineages. Further, connectivity does not follow the often-cited early-to-early, late-to-late model. Instead, the feed-forward motif is formed by sequential addition of temporal cohorts, with circuit output neurons born before circuit input neurons. Further, we generate multiple new tools for the fly community. Ultimately, our data suggest that sequential addition of neurons (with outputs neurons being oldest and input neurons being youngest) could be a fundamental strategy for assembling feed-forward circuits.

developmental biology↗